ZMP

usp54a

Ensembl ID:

ENSDARG00000077948

ZFIN ID:

ZDB-GENE-090828-2

Human Orthologue:

USP54

Human Description:

ubiquitin specific peptidase 54 [Source:HGNC Symbol;Acc:23513]

Mouse Orthologue:

Usp54

Mouse Description:

ubiquitin specific peptidase 54 Gene [Source:MGI Symbol;Acc:MGI:1926037]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35469	Nonsense	Available for shipment	Available now
sa12838	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa35469

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110794	Nonsense	946	1497	17	21

Genomic Location (Zv9):

Chromosome 13 (position 22505095)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	22234433
GRCz11	13	22364883

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTTCCCAGAAGGACAATACAGGGGACCACCCTAGTTCTCTTGATGTGACA[G/T]AAAATGATCGGGGTCCTAGGGACCTTGTAATTAACACAAACTCTCTTGTA

Long Flanking Sequence:

CCTGCTGCTGCCTGCGGTTGTGTATATGTATGCGAGTGTGTGTGTGTGCTCCAGGAGCCTTGCACACAGGAAGAGGAAATGTGCTTTAAAAATTATGATCAGCACTGTTGCAGGCCAGGTTAGATTAAGTAACCATTCTGCAAAGAGCTGCACAGGTAATAGTGTCACCTCTAGACTGAAACAAGTACTGCATGACATTATCAAGACCTGATTCAAGTTAGTCGGATAGATTGTTAGCAGGAACTCATTGCTGTTTTTCATCTTCCTCATTCAGTGAACAGTCTGTCCCGGTCCAAATACTTCTGACAAATGTTAAAGAAGAGGATGAGAAGGCCATTTCAGAAGATGCATTAAGACCACCGTCACCTCTCCACATAAAACCTCAGTCTACAAGTAAACCGATTTCTGAAACCCCAGGCCCTCCTGTCCCCTCTTACCATACAGATACATGTTCCCAGAAGGACAATACAGGGGACCACCCTAGTTCTCTTGATGTGACA[G/T]AAAATGATCGGGGTCCTAGGGACCTTGTAATTAACACAAACTCTCTTGTACAAACTGCTAGTAAACGCAGTCCTGCCACTGTGCCTGTGATTGCAGCGAATGGCTGTGAGGCTTCCCTGCAGTCCTCCGTTTCGCTCAACACTCCTGCTTATTTCAGTGCCCGTCTCACACCTTCCACCACTGATCACTCTGAAGAAGGTCTCCAGAATCCCCATCGTCCTCAGTCTCTCCATGGCCTGTCCCAAGCACCCCATGCCTGTCAAAAATCACTCCCTGTTCCCTCACGTAATTGGTCCTGTCGCAGTCTGGAGCGTCCTGATAGTCGTCCCACCACGCTGGACTCTTCCATGTATTCTCCAGTAGACCTCAGTTCCCCATCGTCCCCCTGTCCTCCATTCCTGTCTTCACCAGTGCTGGAGCAGCGTCCAGCCGGCCCCATGCCTGTGGAACGTTGGGCAGAGAATGTCAATCGATACTACAATTCCCAGAAGTGTGCGCGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa12838

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110794	Nonsense	1105	1497	17	21

Genomic Location (Zv9):

Chromosome 13 (position 22505574)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	22234912
GRCz11	13	22365362

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCCGGCCCCATGCCTGTGGAACGTTGGGCAGAGAATGTCAATCRATACTA[C/A]AATTCCCAGAAGTGTGCGCGGTCGGGACGTGACTCGCCYTGYGAGGAGCT

Long Flanking Sequence:

CCTAGTTCTCTTGATGTGACAGAAAATGATCGGGGTCCTAGGGACCTTGTAATTAACACAAACTCTCTTGTACAAACTGCTAGTAAACGCAGTCCTGCCACTGTGCCTGTGATTGCAGCGAATGGCTGTGAGGCTTCCCTGCAGTCCTCCGTTTCGCTCAACACTCCTGCTTATTTCAGTGCCCGTCTCACACCTTCCACCACTGATCACTCTGAAGAAGGTCTCCAGAATCCCCATCGTCCTCAGTCTCTCCATGGCCTGTCCCAAGCACCCCATGCCTGTCAAAAATCACTCCCTGTTCCCTCACGTAATTGGTCCTGTCGCAGTCTGGAGCGTCCTGATAGTCGTCCCACCACGCTGGACTCTTCCATGTATTCTCCAGTAGACCTCAGTTCCCCATCGTCCCCCTGTCCTCCATTCCTGTCTTCACCAGTGCTGGAGCAGCGTCCAGCCGGCCCCATGCCTGTGGAACGTTGGGCAGAGAATGTCAATCGATACTA[C/A]AATTCCCAGAAGTGTGCGCGGTCGGGACGTGACTCGCCCTGCGAGGAGCTGTCGGAGCTGGACTCACTCTATCAGGCCAGCTTGAAGGCTCCCAGCATACCTAGAGCCACACGGGGAACCAGCCCTCAGCTTGCCAACAGATCAGGTGATTTTTTGTTTTTGTTTAACCTTTTGAAGATACGACTTGTTTTTCACAGGTCATGGAATTTCTGGAGTATCATGGAATATTTTGTTCCAGACATTGAACGTCAGGGATTTTTTTTGTCAGGTCATGGAATATCAGGGGATTTTGTTGGTCACTTTTAAGATTTGTTTCCATTTATTAAAATGTAAATTTTCTATATCATATTTTTGTTATACCATGTTGTTTTTCACAGACATGCAAAAGTCAAAACCAATTTCTTTTTGCTGGCTTTTTTTGTTTTTTTTAATCAGTTAAATTTTCCATTGCGGTTTTCATAGTGGCTCATGCAGTAATCATGCAAATTATTATTCAAGCT

Associated Phenotype:

Not determined